Braunstein, Kerstin E <br/><br/>
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons.  [electronic resource] 

 -  Human molecular genetics  Nov 2010 
 - 4385-98 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddq361  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Atrophy<br/>Behavior, Animal--physiology<br/>Cells, Cultured<br/>Corpus Striatum--metabolism<br/>Dopamine--genetics<br/>Dynactin Complex<br/>Dyneins--genetics<br/>Embryo, Mammalian<br/>Heterozygote<br/>Huntington Disease--genetics<br/>Male<br/>Mice<br/>Mice, Inbred C3H<br/>Microtubule-Associated Proteins--genetics<br/>Nerve Degeneration--genetics<br/>Neurites--metabolism<br/>Neurons--metabolism<br/>Point Mutation<br/>Receptors, Dopamine D2--genetics<br/>Substantia Nigra--metabolism